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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1010577Generated: October 26, 2026

Methane → N-[3-(2-ethoxy-2-hydroxyacetyl)-phenyl]-benzenesulphonamide

https://huagongshe.com/reaction/1010577

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethaneHCID 297—
ReactantWaterHCID 962—
ReactantSelenium DioxideHCID 24007—
Reactant1,4-DioxaneHCID 31275—
ReactantN-(2-acetylphenyl)benzenesulfonamideHCID 3479040—
ProductN-[3-(2-ethoxy-2-hydroxyacetyl)-phenyl]-benzenesulphonamideHCID 5742908046%

Reaction Conditions

Temperature80 °C

Reaction Steps

1 ml of water, 1 g activated charcoal and 2.66 g (24 mmol) selenium dioxide was added to a solution of 1.65 g (6.00 mmol) N-(acetylphenyl)benzenesulphonamide in about 10 mL dioxane. The reaction mixture was stirred for approx. 4 d at 80° C. and then the solvent was eliminated using the rotary evaporator. The residue was dissolved in about 30 ml of ethanol and refluxed for approx. 4 h. The solvent was eliminated from the reaction mixture using the rotary evaporator, the residue was dissolved in about 100 mL ethyl acetate, washed about three times with 30 ml saturated aqueous sodium hydrogen carbonate solution, dried over sodium sulphate and the solvent was eliminated using the rotary evaporator. 0.917 g (2.73 mmol, 46%) N-[3-(2-ethoxy-2-hydroxyacetyl)-phenyl]-benzenesulphonamide were obtained as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977334B2
Source datasetuspto-grants-2011_07
ORD IDord-ef6e5f3802194fe1a97537263c90f728
Source noteuspto-grants-2011_07